AGAPPE Bath Additive - Indonesia BPOM Medical Device Registration
AGAPPE Bath Additive is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204220309. The device is manufactured by AGAPPE DIAGNOSTICS SWITZERLAND GMBH. from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MULTIMEDILAB KARYAMANDIRI.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
AGAPPE DIAGNOSTICS SWITZERLAND GMBH.Country of Origin
Switzerland
Authorized Representative
PT. MULTIMEDILAB KARYAMANDIRIAR Address
GP plaza lantai 3 unit 6, jalan Gelora II No. 01
Registration Date
Nov 08, 2022
Expiry Date
Feb 07, 2027
Product Type
Reagents and Specimen Providers
General purpose reagent.
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